部分構造検索

946397

COc1ccc(C(OC[C@H]2O[C@@H](n3cc(C)c(=O)[nH]c3=O)C[C@@H]2O)(c2ccccc2)c2ccc(OC)cc2)cc1
Reaction #3746
5
収率 85.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(OC[C@H]2O[C@@H](n3cc(C)c(=O)[nH]c3=O)C[C@@H]2O[Si](C)(C)C(C)(C)C)(c2ccccc2)c2ccc(OC)cc2)cc1
Reaction #3747
5'-O-(4,4'-dimethoxytrityl)-3'-O-(tert-butyldimethlsilyl) thymidine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cn([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O2)c(=O)[nH]c1=O
Reaction #3748
3'-O-(tert-butyldimethylsilyl) thymidine
収率 92.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(OC[C@@]2(COS(=O)(=O)c3ccc(C)cc3)O[C@@H](n3cc(C)c(=O)[nH]c3=O)[C@H](O)[C@H]2OCc2ccccc2)(c2ccccc2)c2ccc(OC)cc2)cc1
Reaction #6875
nucleoside
収率 75.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(OC[C@@]23CO[C@@H]([C@H](n4cc(C)c(=O)[nH]c4=O)O2)[C@H]3OCc2ccccc2)(c2ccccc2)c2ccc(OC)cc2)cc1
Reaction #6876
nucleoside
収率 96.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cn([C@@H]2O[C@@]3(CO)CO[C@@H]2[C@H]3O)c(=O)[nH]c1=O
Reaction #6877
nucleoside
収率 82.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(OC[C@@]23CO[C@@H]([C@H](n4cc(C)c(=O)[nH]c4=O)O2)[C@H]3O)(c2ccccc2)c2ccc(OC)cc2)cc1
Reaction #6878
nucleoside
収率 50.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC=CCCOc1ccc(C(OCC2OC(n3cc(C)c(=O)[nH]c3=O)CC2O)(c2ccccc2)c2ccc(OCCC=CC=C)cc2)cc1
Reaction #180134
DOI: 10.1039/C8SC04228D
COc1ccc(C(OCC2OC(n3cc(C=CBr)c(=O)[nH]c3=O)CC2OC)(c2ccccc2)c2ccc(OC)cc2)cc1
Reaction #269384
DOI: 10.1039/C8SC04228D
COc1ccc(C(OCC2(C=CCCCCCNC(=O)C(F)(F)F)OC(n3cc(C)c(=O)[nH]c3=O)CC2O[SiH2]C(C)(C)C(C)C)(c2ccccc2)c2ccc(OC)cc2)cc1
Reaction #378411
DOI: 10.1039/C8SC04228D
COc1ccc(C(OC[C@H]2O[C@@H](n3cc(C)c(=O)[nH]c3=O)C[C@@]2(O)CN=[N+]=[N-])(c2ccccc2)c2ccc(OC)cc2)cc1
Reaction #439176
5′-O-(4,4′-dimethoxytrityl)-3′-C-azidomethylthymidine
収率 92.0%DOI: 10.6084/m9.figshare.5104873.v1
COC1(OC)C=CC(C(OC[C@H]2O[C@@H](n3cc(C)c(=O)[nH]c3=O)C[C@@]23CO3)(c2ccccc2)c2ccccc2)=CC1
Reaction #439177
5′-O-(4,4-dimethoxytrityl)-3′-C,O-methylene thymidine
収率 8.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(OC[C@H]2O[C@@H](n3cc(C)c(=O)[nH]c3=O)C[C@]2(C)O)(c2ccccc2)c2ccc(OC)cc2)cc1
Reaction #439178
5′-O-(4,4′-dimethoxytrityl)-3′-C-methylthymidine
収率 79.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(OC[C@H]2O[C@@H](n3cc(C)c(=O)[nH]c3=O)C[C@@]2(O)CN)(c2ccccc2)c2ccc(OC)cc2)cc1
Reaction #439179
5′-O-(4,4′-dimethoxytrityl)-3′-C-aminomethylthymidine
収率 45.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cn([C@H]2C[C@H](OC(=O)OCC(C)c3ccccc3[N+](=O)[O-])[C@@H](CO)O2)c(=O)[nH]c1=O
Reaction #441395
title compound
収率 93.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(COC(=O)O[C@H]2C[C@H](n3cc(C)c(=O)[nH]c3=O)O[C@@H]2CO)c([N+](=O)[O-])cc1OC
Reaction #441398
title compound
収率 66.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC=CCCOc1ccc(C(OC[C@H]2O[C@@H](n3cc(C)c(=O)[nH]c3=O)C[C@@H]2O)(c2ccccc2)c2ccc(OCCC=CC=C)cc2)cc1
Reaction #450728
compound 31
収率 84.4%DOI: 10.6084/m9.figshare.5104873.v1
C=CC=CCCOc1ccc(C(OC[C@H]2O[C@@H](n3cc(C)c(=O)[nH]c3=O)C[C@@H]2OP(N)O)(c2ccccc2)c2ccc(OCCC=CC=C)cc2)cc1
Reaction #450729
compound 32
収率 85.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(OC[C@H]2O[C@@H](n3cc(C)c(=O)[nH]c3=O)C[C@@H]2O)(c2ccccc2)c2ccc(OC)cc2)cc1
Reaction #465721
5
収率 85.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(OC[C@H]2O[C@@H](n3cc(C)c(=O)[nH]c3=O)C[C@@H]2O[Si](C)(C)C(C)(C)C)(c2ccccc2)c2ccc(OC)cc2)cc1
Reaction #465722
5'--O--(4,4'-dimethoxytrityl)-3'--O--(tert-butyldimethylsilyl) thymidine
DOI: 10.6084/m9.figshare.5104873.v1
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